Aroyl ketone derivative, UV ray absorber comprising the same, and cosmetic composition containing the same

ABSTRACT

A novel aroyl ketone derivative represented by formula (I) is disclosed. 
     
         Ar(COCH.sub.2 COR.sup.1).sub.n                             (I) 
    
     wherein R 1  represents a saturated or unsaturated hydrocarbon group having 1-24 carbon atoms, or a linear or branched alkoxyalkyl or alkenyloxyalkyl group having 1-24 carbon atoms, dialkylamino group having 1-24 carbon atoms, Ar represents a benzene or naphthalene ring which may be substituted with one or more hydroxyl groups, alkoxy groups having 1-24 carbon atoms, alkenyloxy groups having 1-24 carbon atoms, polyoxyleneoxy groups, mono- or dialkyl amino groups having 1-24 carbon atoms, or α-methylenedioxy groups, and n denotes an integer of 1-4. An UV-ray absorber and cosmetic composition comprising the aroyl ketone derivative of formula (I) are also disclosed. Aroyl ketone derivative (I) of the present invention can provide an excellent UV-ray absorbing effect and has outstanding stability against light, and the UV-ray absorber or cosmetic composition containing the aroyl ketone derivative (I) can exhibit an excellent sunscreening effect.

RELATED APPLICATIONS

This application is a continuation-in-part application of applicationSer. No. 07/577,567 filed on Sep. 5, 1990 now abandoned.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a novel aroyl ketone derivative possessingUV-ray absorbing ability and outstanding stability against light, and toa UV-ray absorber and a cosmetic composition both containing such anaroyl ketone derivative and exhibiting a superior effect of protectingthe skin from sunburn.

2. Description of the Background Art

Ultraviolet rays are known to cause various changes to the skin. Indermatology, UV-rays are classified into (a) long wavelength UV-rays of400-320 nm, (b) medium wavelength UV-rays of 320-290 nm, and (c) shortwavelength UV-rays of less than 290 nm. These are called UV-A, UV-B, andUV-C, respectively. The UV-rays contained in the sunlight are UV-A andUV-B, whereas UV-C is absorbed in the ozone layer and therefore scarcelyreaches the ground.

The UV-B, when irradiated onto the skin in an amount exceeding a certainlevel, causes red spots or blisters on the skin. In addition, the UV-Btends to promote the formation of melanin, resulting in the melanoses orother adverse changes of the skin. On the other hand, UV-A inducesmelanism on the skin immediately after irradiation (instantaneousmelanism). In addition, UV-A energy reaches the corium and brings aboutchronic changes in the blood vessel walls and the elastic fibers inconnective tissues. Such behaviors of both UV-A and UV-B are consideredto accelerate aging of the skin and to be a cause of wrinkles, spots orfreckles.

As such effects of UV-rays on human skin have been clarified, variouschemical compounds capable of absorbing UV-A and/or UV-B have beendeveloped. Such UV-ray absorbers are desired to satisfy the followingrequirements (1) through (5):

(1) absorbing UV-A or UV-B light to the maximum.

(2) having good stability against heat and light.

(3) being free from toxicity, irritation, and any other harmful actionsto the skin.

(4) having a long-lasting effect.

(5) having an excellent compatibility with cosmetic base materials.

Conventionally, for example, dibenzoylmethane derivatives are used as aUV-A absorber; and derivatives of cinnamate, benzophenone,p-aminobenzoic acid, salicylic acid, and the like are used as a UV-Babsorber.

However, these conventional UV-ray absorbers can not necessarily satisfythe above requirements. Specifically, these UV-ray absorbers are knownto be inadequate in the stability against light and to decompose orreact by UV-ray irradiation (Int. J. Cosmetic Science, 10, 53, 1988).Such decomposition of UV-ray absorbers substantially decreases thelasting effect of compositions. Adverse effects to the skin resultingfrom decomposed substances themselves or compounds produced by thereaction of the decomposed substances and other components can not beneglected (Fragrance Journal, 84, 34, 1987).

Development of improved UV-ray absorbers which satisfy the abovecharacteristics, especially UV-ray absorbers having excellent stabilityagainst light, has therefore been desired.

The inventors have synthesized many diketone derivatives and examinedtheir characteristics, and, as a result, found that an aroyl ketonederivative represented by formula (I) shown below had an outstandingUV-A and UV-B absorbing ability and excellent stability against light,and further found that a cosmetic composition comprising the aroylketone derivative could efficiently protect the skin from beingsunburnt.

SUMMARY OF THE INVENTION

Accordingly, an object of this invention is to provide a novel aroylketone derivative represented by the following formula (I):

    Ar(COCH.sub.2 COR.sup.1).sub.n                             (I)

will hereinafter become more readily apparent from the followingdescription.

DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS

Enumerated as examples of R¹ having 1-24 carbon atoms, saturated orunsaturated, are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl,t-butyl, butenyl, n-pentyl, n-hexyl, n-heptyl, heptenyl, n-octyl,octenyl, n-nonyl, nonenyl, n-decyl, decenyl, n-undecyl, undecenyl,n-dodecyl, dodecenyl, n-tridecyl, tridecenyl, n-tetradecyl,tetradecenyl, n-pentadecyl, pentadecenyl, isopentadecyl, n-hexadecyl,hexadecenyl, isohexadecyl, n-heptadecyl, heptadecenyl, isoheptadecyl,n-octadecyl, octadecenyl, isooctadecyl, cyclohexyl, and adamantyl groupsand the like. Enumerated as examples of hydroxyalkyl groups having 1-18carbon atoms are hydroxymethyl, hydroxyethyl, hydroxypropyl,hydroxybutyl, hydroxypentyl, hydroxyhexyl, hydroxyheptyl, hydroxyoctyl,hydroxynonyl, hydroxydecyl, hydroxyundecyl, hydroxydodecyl,hydroxytetradecyl, hydroxyhexadecyl, hydroxyoctadecyl groups and thelike. Enumerated as examples of linear or branched alkoxyalkyl groupshaving 1-24 carbon atoms are methoxymethyl, ethoxymethyl, propoxymethyl,isopropoxymethyl, butoxymethyl, pentyloxymethyl, hexyloxymethyl,octyloxymethyl, decyloxymethyl, undecyloxymethyl, tetradecyloxymethyl,hexadecyloxymethyl, octadecyloxymethyl, methoxyethyl, ethoxyethyl,allyloxyethyl, propoxyethyl, methoxypropyl,

    Ar(COCH.sub.2 COR.sup.1).sub.n                             (I)

wherein R¹ represents a saturated or unsaturated hydrocarbon grouphaving 1-24 carbon atoms, or a linear or branched alkoxyalkyl oralkenyloxyalkyl group having 1-24 carbon atoms, dialkylamino grouphaving 1-24 carbon atoms, Ar represents a benzene or naphthalene ringwhich may be substituted with one or more hydroxyl groups, alkoxy groupshaving 1-24 carbon atoms, alkenyloxy groups having 1-24 carbon atoms,mono- or dialkyl amino groups having 1-24 carbon atoms, orα-methylenedioxy groups, and n denotes an integer of 1-4.

Still another object of this invention is to provide a cosmeticcomposition comprising an aroyl ketone derivative represented by thefollowing formula (I):

    Ar(COCH.sub.2 COR.sup.1).sub.n                             (I)

wherein R¹ represents a saturated or unsaturated hydrocarbon grouphaving 1-24 carbon atoms, or a linear or branched alkoxyalkyl oralkenyloxyalkyl group having 1-24 carbon atoms, Ar represents a benzeneor naphthalene ring which may be substituted with one or more hydroxylgroups, alkoxy groups having 1-24 carbon atoms, alkenyloxy groups having1-24 carbon atoms, mono- or dialkyl amino groups having 1-24 carbonatoms, or α-methylenedioxy groups, and n denotes an integer of 1-4.

Other objects, features and advantages of the invention wherein R¹represents a saturated or unsaturated hydrocarbon group having 1-24carbon atoms, or a linear or branched alkoxyalkyl or alkenyloxyalkylgroup having 1-24 carbon atoms, dialkylamino group having 1-24 carbonatoms, Ar represents a benzene or naphthalene ring which may besubstituted with one or more hydroxyl groups, alkoxy groups having 1-24carbon atoms, alkenyloxy groups having 1-24 carbon atoms, mono- ordialkyl amino groups having 1-24 carbon atoms, or α-methylenedioxygroups, and n denotes an integer of 1-4; excluding the compoundsrepresented by the following formulae: ##STR1##

Another object of the present invention is to provide a UV-ray absorbercomprising an aroyl ketone derivative represented by the followingformula (I): ethoxypropyl, allyloxypropyl, propoxypropyl, methoxybutyl,ethoxybutyl, allyloxybutyl, propoxybutyl, methoxypentyl, ethoxypentyl,allyloxypentyl, propoxypentyl, methoxydodecyl, ethoxydodecyl,allyloxydodecyl, propoxydodecyl, methoxyhexadecyl, ethoxyhexadecyl,allyloxyhexadecyl, propoxyhexadecyl, methoxyhexadecyl, ethoxyoctadecyl,allyloxyoctadecyl, propoxyoctadecyl groups, and the like. Given asexamples of alkenyloxyalkyl groups having 1-24 carbon atoms areallyloxymethyl, butenyloxymethyl, hexenyloxymethyl, undecenyloxymethyl,octadecenyloxymethyl groups, and the like. Enumerated as examples ofdialkylamino groups having 1-24 carbon atoms are dimethylamino,ethylmethylamino, diethylamino, methylpropylamino, methylisopropylamino,methylbutylamino, methyl-t-butylamino, diisopropylamino, dipropylamino,ethylbutylamino, methylhexylamino, di-sec-butylamino, diisobutylamino,dipentylamino, dihexylamino, bis 2-ethylhexylamino, dioctylamino,methyloctadecylamino, pyrrolidyl, piperidyl, morpholinyl groups, and thelike.

Preferable examples of linear or branched alkoxy groups having 1-24carbon atoms, by which the benzene or naphthalene ring (Ar) may besubstituted, are those having 1-8 carbon atoms, for example, methoxy,ethoxy, n-propoxy, isopropoxy, n-butoxy, and tert-butoxy groups, and thelike. Preferable examples of alkenyloxy groups having 1-24 carbon atoms,by which the benzene or naphthalene ring (Ar) may be substituted, arethose having 1-8 carbon atoms, for example, allyloxy, butenyloxy,pentenyloxy and hexenyloxy groups, and the like. Preferable examples ofmono- or dialkyl amino groups having 1-24 carbon atoms, by which thebenzene or naphthalene ring (Ar) may be substituted, are those having1-8 carbon atoms, for example, dimethylamino, diethylamino anddiisopropyl groups, and the like.

n is an integer of 1-4, but its preferable range is 1-3.

Aroyl ketone derivative (I) of the present invention can be produced byone of the following processes (a), (b) or (C), according to knownmethods, for example, reported in J. Am. Chem. Soc., 80, 4891, (1958);J. Chromatogr., 312, 109, (1984); and J. Polym. Sci. Polym. Chem. Ed.,20, 3079, (1982). ##STR2## wherein R² represents a methyl group, ethylgroup, n-propyl group, or a n-butyl group and R¹ and n have the samemeanings as defined above.

As is clear from the above reaction scheme, compound (I) of the presentinvention can be prepared by condensation of an ester of formula (II)and a ketone of formula (III). In process (a), it is desirable that thereaction be carried out at 20°-150° C. for tens of minutes to 10 hoursin a solvent ##STR3## X is oxygen.

As is clear from the above reaction scheme, compound (I) of the presentinvention can be prepared by condensation of an ester of formula (II)and an acetoamide of formula (IV). The reaction of process (c) can becarried out under the same conditions as in process (a).

The UV-ray absorbing agent of the present invention may consist of oneor more aroyl ketone derivatives of formula (I) thus obtained. However,it is more desirable to use the aroyl ketone derivatives of the presentinvention mixed with a carrier. Any kind of carriers which are inert tothe aroyl ketone derivative (I) of the present invention and in the formeither of solid, liquid, emulsion, foam, gel, or the like can be used.Typical examples of these carriers are water; alcohols; oil and fats,e.g. hydrocarbon oils, fatty acid esters, long-chain alcohols, silicone;micro powders of starch, talc, and the like; low boiling pointhydrocarbons or halogenated hydrocarbons used as an conventional aerosolpropellant; and the like. In addition to the above components, anyconventional components may be incorporated in the UV-ray absorber ofthe present invention to the extent that the UV-ray absorbing effect ofthe aroyl ketone derivative of the present invention will not beimpaired. These conventional components include, for example,antiseptics, perfumes, pigments, surfactants, and the like. such asanhydrous tetrahydrofuran, toluene, xylene, or the like using a base asa catalyst. The base used in this process is a metallic hydride, e.g.sodium hydride; an alkyl metal, e.g. butyl lithium; an amine, e.g.triethylamine; a metal amide, e.g. sodium amide; a metal alkoxide, e.g.sodium methoxide; and the like. ##STR4## wherein R¹, R², and n have thesame meanings as defined above.

As is clear from the above reaction scheme, compound (I) of the presentinvention can be prepared by condensation of an acetylbenzene derivativeor an acetylnaphthalene derivative of formula (IV) and an ester offormula (V). The reaction of process (b) can be carried out under thesame conditions as in process (a). ##STR5## wherein R¹, R², and n havethe same meanings as defined above. R³ and R⁴ each represents ahydrocarbon group having 1-18 carbon atoms, which may form a ring suchas,

The cosmetic compositions containing the aroyl ketone derivative (I) ofthe present invention (hereinafter designated as "cosmetic compositionof the present invention") can be produced by incorporating one or morearoyl ketone derivatives (I) having compatibility with the basecomponents of the cosmetic composition according to a conventionalmethod. The cosmetic composition can be prepared into various forms suchas creams, liquids, oils, sprays, sticks, emulsions, foundations,ointments, and the like.

The selective use of aroyl ketone derivatives (I) which are compatiblewith the cosmetic bases ensures preparation of cosmetic compositionshaving UV-ray absorbing effect of various types, for example,fundamental cosmetics such as cosmetic oils with oil bases, oil creamsand milky lotions with a large quantity of oil, weakly oily creams andlotions, water-base lotions; and make-up cosmetics such as oil-basefoundations, lipsticks. Examples of these base components or solventsuseful for the cosmetic compositions of the present invention arehydrocarbons such as solid or liquid paraffins, crystal oils, ceresin,ozokerite, montan wax, and the like; oils, fats, or waxes of plant oranimal origin such as olive oil, earth wax, carnauba wax, lanolin,spermaceti, and the like; fatty acids and esters thereof such as stearicacid, palmitic acid, oleic acid, glycerol monostearate, glyceroldistearate, glycerol monooleate, isopropyl myristate, isopropylstearate, butyl stearate, and the like; alcohols such as ethyl alcohol,isopropyl alcohol, cetyl alcohol, stearyl alcohol, palmityl alcohol,hexyldodecyl alcohol, and the like. In addition, polyhydric alcoholshaving a moisturizing effect such as glycol, glycerol, sorbitol, and thelike may also be used.

The amount of aroyl ketone derivative (I) to be incorporated in theUV-ray absorbing agent or cosmetic composition of the present inventionvaries depending on their types or forms of products. There are nospecific limitations as to the amount to be added in inasmuch as such anaddition brings about the effect of the present invention. A preferableamount is 0.1-20% by weight, and particularly 0.5-10% by weight, of thecrude product.

The UV-ray absorbing agent or cosmetic composition of the presentinvention can be prepared by simply incorporating the aroyl ketonederivative (I) as a UV-ray absorber. However, it is more preferable toprovide a sunscreen cosmetics for general use by incorporatingconventional UV-A or UV-B absorbers together with the aroyl ketonederivative (I) of this invention. Examples of these conventional UV-Babsorbers include, p-methylbenzylidene-D,L-camphor or its sodiumsulfonate, sodium 2-phenylbenzimidazole-5-sulfonate, sodium3,4-dimethylphenylglyoxylate, 4-phenylbenzophenone, isooctyl4-phenylbenzophenone-2'-carboxylate, p-methoxycinnamate,2-phenyl-5-methylbenzoxazol, p-dimethylaminobenzoate, and the like.Examples of the UV-A absorbers are 4-methoxy-2'-carboxydibenzoylmethane,4-methoxy-4'-t-butyldibenzoyl-methane, 4-isopropyldibenzoylmethane,2-hydroxy-4-methoxybenzophenone, dibenzylidenecamphor, and the like.

Into the cosmetic compositions of the present invention, variousadditives other than the above-mentioned components can be incorporated.Suitable additives are, for example, W/O and O/W emulsifiers which areavailable in the market; and viscosity increasing agents such asmethyl-, ethyl-, or carboxymethyl cellulose, polyacrylic acid,tragacanth, agar, gelatin, and the like. As required, perfumes,antiseptics, humectants, emulsion stabilizers, medical components,and/or coloring agents which are physiologically acceptable, may also beformulated into the cosmetic composition of this invention.

Other features of the invention will become apparent in the course ofthe following description of the exemplary embodiments which are givenfor illustration of the invention and are not intended to be limitingthereof.

EXAMPLES Example 1 Synthesis of3,4-dimethoxyphenyl-4,4-dimethylpentane-1,3-dione

In a 200 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitrogen-inlet tube, 2.45 gm(61 mmol) of 60% sodium hydride, 10 gm (51 mmol) of methyl3,4-dimethoxybenzoate, and 100 ml of anhydrous tetrahydrofuran weremixed with stirring under nitrogen stream, and refluxed with heatingwhile 6.1 gm (61 mmol) of pinacolone was added dropwise. The refluxingunder heat was continued for 7 hours. After cooling the reactionmixture, 30 ml of 2N hydrochloric acid was added and the mixture wasextracted twice with chloroform. The extract was dried over anhydroussodium sulfate and the solvent was removed by evaporation to give acrude product. Hexane was added to the crude product and insolublesubstances were filtered off. The filtrate was concentrated byevaporation, and recrystallization afforded 8.9 gm of the targetcompound as colorless needles (yield: 65%).

Melting Point: 52.3°-53.3° C.

IR(ν_(KBr), cm⁻¹): 1600, 1520, 1470, 1450, 1370, 1300, 1270, 1220, 1190,1130, 890, 709, 730,

¹ H-NMR(CDCl₃, δ): 1.26(9H, s, t-C₄ H₉), 3.95(3H, s, OCH₃), 3.96(3H, s,OCH₃), 6.24(1H, s), 6.90(1H, d, J=8.4Hz), 7.49(1H, s) 7.51(1H, d,J=8.4Hz)

Elemental analysis Calculated (%) C: 68.16, H: 7.63 Found (%) C: 68.23,H: 7.60.

Example 2 Synthesis of3,4,5-trimethoxyphenyl-4,4-dimethylpentane-1,3-dione

In a 200 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 3.0 gm (75mmol) of 60% sodium hydride, 10 gm (44.3 mmol) of methyl3,4,5-trimethoxybenzoate, and 80 ml of anhydrous tetrahydrofuran weremixed with stirring under nitrogen stream, and refluxed with heatingwhile 5.3 gm (53.2 mmol) of pinacolone was added dropwise. Refluxingunder heat was continued for 5 hours. After cooling the reactionmixture, 45 ml of 2N hydrochloric acid was added, the mixture wasextracted twice with chloroform. The extract was dried over anhydroussodium sulfate and the solvent was removed by evaporation to give acrude product. Hexane was added to the crude product and insolublesubstances were filtered off. The filtrate was concentrated byevaporation, and recrystallization afforded 9.6 gm of the targetcompound as colorless needles (yield: 74%).

Melting Point: 67.3°-68.4° C.

IR(ν_(KBr), cm⁻¹): 2970, 1590, 1560, 1510, 1470, 1430, 1340, 1230, 1220,1180, 1130, 990, 800.

¹ H-NMR(CDCl₃, δ): 1.26(9H, s, t-C₄ H₉), 3.91(3H, s, OCH₃), 3.93(6H, s,OCH₃), 6.21(1H, s), 7.13(2H, s),

Elemental analysis Calculated (%) C: 65.29, H: 7.53 Found (%) C: 65.38,H: 7.51.

Example 3 Synthesis of 1,4-bis(4,4-dimethyl-3-oxopentanoyl)-benzene

In a 2 1 four-necked flask equipped with a mechanical stirrer, droppingfunnel, thermometer, reflux condenser, and a nitrogen-inlet tube, 32 gm(0.8 mol) of 60% sodium hydride, 79 gm (0.79 mol) of pinacolone, and 700ml of anhydrous tetrahydrofuran were mixed with stirring under nitrogenstream. To this solution, 70 gm (0.36 mol) of dimethylterephthalate in300 ml of tetrahydrofuran was added dropwise over one hour. After theaddition, the reaction mixture was refluxed with heating for 6 hours,and was cooled to room temperature. After addition of 180 ml of 2Naqueous hydrochloric acid, the reaction mixture was extracted withchloroform. The extract was dried over anhydrous sodium sulfate and thesolvent was evaporated to give a crude product. The crude product wasrecrystallized using hexane to obtain 78 gm of the target compound ascolorless scales (yield: 66%).

Melting Point: 125.5°-126.5° C.

IR(ν_(KBr), cm⁻¹): 2974, 2872, 1584, 1563, 1485, 1368, 1290, 1140, 840,792, 741.

¹ H-NMR(CDCl₃, δ): 1.27(18H, s , 6.34(2H, s), 7.95(4H, s)

Elemental analysis Calculated (%) C: 72.70, H: 7.93 Found (%) C: 72.61,H: 7.96.

Example 4

Synthesis of 1,3-bis(4,4-dimethyl-3-oxopentanoyl)-benzene

In a 100 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 1.5 gm (38mmol) of 60% sodium hydride, 3.6 gm (36 mmol) of pinacolone, 3.0 gm(15.5 mmol) of dimethyl isophthalate, and 30 ml of anhydroustetrahydrofuran were mixed with stirring under nitrogen stream andrefluxed with heating for 6 hours. After cooling the reaction mixture,10 ml of 2N aqueous hydrochloric acid was added the product wasextracted with chloroform. The extract was dried over anhydrous sodiumsulfate and the solvent was evaporated to give a crude product.Recrystallization using hexane afforded 3.1 gm of the target compound ascolorless crystals (yield: 61%).

Melting Point: 106.0°-107.5° C.

IR(ν_(KBr), cm⁻¹): 3124, 2974, 2872, 1611, 1563, 1482, 1431, 1290, 1227,1134, 1095, 879, 804, 705.

¹ H-NMR(CDCl₃, δ): 1.27(18H, br.s), 6.34(2H, s), 7.55(1H, br.t,J=7.8Hz), 8.00 and 8.04(2H, dd, J=7.8Hz, J=1.5Hz), 8.38(1H, br.s).

Elemental analysis Calculated (%) C: 72.70, H: 7.93 Found (%) C: 72.58,H: 7.95.

Example 5 Synthesis of4-methoxy-1,3-bis(4,4-dimethyl-3-oxopentanoyl)benzene

In a 100 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 1.5 gm (38mmol) of 60% sodium hydride, 3.6 gm (36 mmol) of pinacolone, 3.0 gm(13.4 mmol) of dimethyl 4-methoxyisophthalate, and 30 ml of anhydroustetrahydrofuran were mixed with stirring under nitrogen stream andrefluxed with heating for 5 hours. After cooling the reaction mixture,10 ml of 2N aqueous hydrochloric acid was added, and the product wasextracted with chloroform. The extract was dried over anhydrous sodiumsulfate and the solvent was removed by evaporation. The crude productwas recrystallized using hexane to obtain 3.2 gm of the target compoundas colorless crystals (yield: 66%).

Melting Point: 69.4°-70.8° C.

IR(ν_(KBr), cm⁻¹): 2968, 1620, 1584, 1506, 1467, 1368, 1275, 1263, 1182,1131, 1071, 1011, 795.

¹ H-NMR(CDCl₃, δ): 1.24(9H, s), 1.25(9H, s), 3.99(3H, s), 6.29(1H, s),6.52(1H, s), 7.04(1H, d, J=8.8Hz), 8.04(1H, dd, J=2.3Hz, J=8.8Hz),8.35(1H, d, J=2.3Hz),

Elemental analysis Calculated (%) C: 69.98, H: 7.83 Found (%) C: 69.92,H: 7.85.

Example 6

Synthesis of 2,6-bis(4,4-dimethyl-3-oxopentanoyl)-naphthalene

To 2.0 gm of dimethyl 2,6-naphthalene dicarboxylate and 2.8 gm ofpinacolone, which had been dissolved in 25 ml of anhydroustetrahydrofuran, 1.1 gm of 60% sodium hydride was added. The mixture wasreacted at 60° C. for 4 hours while stirring. The reaction mixture waspoured into ice-cooled 2N hydrochloric acid. Organic substances wereextracted using chloroform and, after evaporating the solvent,recrystallized in a mixed solvent of chloroform-methanol to obtain 2.1gm of the target compound as pale yellow

Melting Point: 195°-196° C.

IR(ν_(KBr), cm⁻¹): 2968, 2936, 2872, 1618, 1580, 1512, 1480, 1430, 1182,1154, 1128, 1070, 1018, 910, 812, 710, 474.

¹ H-NMR(CDCl₃, δ): 15.81(2H, s , 8.62(2H, s), 7.94-8.10(4H, m), 6.47(2H,s), 1.30(18H, s).

Example 7 Synthesis of 1,4-bis(4-methyl-3-oxopentanoyl)-benzene

The procedures in Example 3 were repeated under substantially sameconditions except that 68 gm (0.79 mol) of isopropylmethylketone wasused instead of 79 gm (0.79 mol) of pinacolone, and afforded 76 gm ofthe target compound as pale yellow needles (Yield: 72%).

Melting Point: 97.0°-97.5° C.

IR(ν_(KBr), cm⁻¹): 2980, 2932, 1608, 1437, 1284, 1188, 1098, 939, 807.

¹ H-NMR(CDCl₃, δ): 1.25(12H, d), 2.55-2.77(2H, m), 6.25(2H, s), 7.95(4H,s), 14.7(2H, bs).

Example 8 Synthesis of 1,4-bis(3-oxopentanoyl)benzene

The procedures in Example 3 were repeated under substantially sameconditions except that 57 gm (0.79 mol) of methylethylketone was usedinstead of 79 gm (0.79 mol) of pinacolone, and afforded 54 gm of thetarget compound as pale yellow crystals (Yield: 56%).

Melting Point: 122.5°-123.5° C.

IR(ν_(KBr), cm⁻¹): 2980, 2950, 1617, 1293, 1161, 1119, 1083, 813, 774.

¹ H-NMR(CDCl₃, δ): 1.25(6H, t), 2.50(4H,q), 6.22(2H, s), 7.95(4H, s),15.2(2H, bs),

Example 9 Synthesis of 1,4-bis(3-oxododecanoyl)benzene

In a 100 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 1.1 gm (28mmol) of 60% sodium hydride, 2.0 gm (12.3 mmol) of p-diacetylbenzene,4.8 gm (25.7 mmol) of methylcaprylate, and 20 ml of anhydroustetrahydrofuran were mixed with stirring under nitrogen stream and therefluxing under heat was continued for 5 hours. After cooling thereaction mixture, 15 ml of 2N aqueous hydrochloric acid was added, andthe mixture was extracted with chloroform. The extract was dried overanhydrous sodium sulfate and the solvent was removed by evaporation togive a crude product. Hexane was added to the crude product andrecrystallization afforded 3.6 gm of the target compound as pale yellowscales (yield: 63%).

Melting Point: 122.5°-123.0° C.

IR(ν_(KBr), cm⁻¹): 2920, 2854, 1617, 1473, 1293, 1155, 786.

¹ H-NMR(CDCl₃, δ):1.90(6H, t), 1.12-1.43(20H, m), 1.56(4H, bs),1.60-1.80(4H,m), 2.47(4H, t), 6.20(2H, s), 7.95(4H, s), l4.6(2H, bs).

Example 10 Synthesis of 1,3,5-tris(4,4-dimethyl-3-oxopentanoyl)-benzene

In a 100 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 2.29 gm (57mmol) of 60% sodium hydride, 5.24 gm (52 mmol) of pinacolone, 4.0 gm(15.8 mmol) of trimethyl-1,3,5-benzenetricarboxylate, and 40 ml ofanhydrous tetrahydrofuran were mixed with stirring under nitrogenstream, and the refluxing under heat was continued for 7 hours. Aftercooling the reaction mixture, 30 ml of 2N aqueous hydrochloric acid wasadded, and the mixture was extracted with chloroform. The extract wasdried over anhydrous sodium sulfate and the solvent was removed byevaporation to give a crude product. Acetone was added to the crudeproduct, and recrystallization afforded 3.8 gm of the target compound asyellow crystals (yield: 52%).

¹ H-NMR(CDCl₃, δ): 1.30(27H, s), 6.41(3H, s), 8.49(3H, s), 15.6(3H, bs).

Example 11 Synthesis of1,4-bis(4-hydroxy-4-methyl-3-oxopentanoyl)benzene

In a 200 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 15 gm (147mmol) of 3-methyl-3-hydroxy-2-butanone, 500 mg (2.0 mmol) of pyridiniump-toluenesulfonate and 100 ml of anhydrous methylenechloride were mixedwith stirring under nitrogen stream, and 11.7 gm (162 mmol) of ethylvinyl ether was added dropwise at room temperature for 3 hours whilestirring. After the reaction, the reaction mixture was washed with 5%aqueous sodium hydrogen carbonate, and then the mixture was extractedwith chloroform. The extract was dried over anhydrous sodium sulfate andthe solvent was removed by evaporation to give a crude product.Distillation of the crude product afforded 17.09 gm of3-(1-ethoxyethoxy)-3-methyl-butane-2-one (b.p. 38-40/l mmHg, yield:66%).

In a 100 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 9.9 gm (57mmol) of above-mentioned 3-(1-ethoxyethoxy)-3-methyl-butane-2-one, 2.3gm (57 mmol) of 60% sodium hydride, 5.0 gm (25 mmol) ofdimethylterephthalate and 50 ml of anhydrous tetrahydrofuran were mixedwith stirring under nitrogen stream, and the refluxing under heat wascontinued for 7 hours. After cooling the reaction mixture, 30 ml of 2Nhydrochloric acid was added and the mixture was extracted withchloroform. The extract was dried over anhydrous sodium sulfate and thesolvent was removed by evaporation. The reaction mixture was stirred atroom temperature while adding 30 ml of methnol with ten drops of 2Nhydrochloric acid. A mixed solvent of acetone-chloroform was added tothe crude product, and recrystallization afforded 4.1 gm of the titlecompound as pale yellow crystals (yield: 48%).

Melting Point: 276.5°-277.5° C.

IR(ν_(KBr), cm⁻¹): 3112, 2980, 1690, 1583, 1425, 1356, 1173, 1056, 825.

¹ H-NMR(CDCl₃, δ): 1.52(12H, s), 6.09(2H, s), 7.95(4H, s), 14.8(2H, bs).

Example 12 Synthesis of 1,4-bis(4-methyl-3-oxo-4-azapentanoyl)-benzene

In a 200 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 5.0 gm (125mmol) of 60% sodium hydride, 10.6 gm (122 mmol) of dimethylacetoamide,10 gm (51 mmol) of dimethylterephthalate and 100 ml of anhydroustetrahydrofuran were mixed with stirring under nitrogen stream, and therefluxing under heat was continued for 4 hours. After cooling thereaction mixture, 65 ml of 2N aqueous hydrochloric acid was added andthe mixture was extracted with chloroform. The extract was dried overanhydrous sodium sulfate and the solvent was removed by evaporation togive a crude product. A mixed solvent of chloroform-ethanol was added tothe crude product, and recrystallization afforded 10.0 gm of the targetcompound as yellow crystals (yield: 64%).

Melting Point: 188.0°-189.0° C.

IR(ν_(KBr), cm⁻¹): 2932, 1620, 1500, 1440, 1360, 1125, 786, 640.

¹ H-NMR(CDCl₃, δ): 3.10(12H, s), 4.13(0.4H, s), 5.88(1.6H, s),7.82(3.2H, s), 7.75(0.4H, d), 8.05(0.4H, d).

Example 13 Synthesis of1-(4-methyl-3-oxo-4-azapentanoyl)-4-(4,4-dimethyl-3-oxopentanoyl)benzene

In a 100 ml three-necked flask equipped with a mechanical stirrer,dropping funnel, reflux condenser, and a nitogen-inlet tube, 5.0 gm (125mmol) of 60% sodium hydride, 5.1 gm (51 mmol) of pinacolone, 10 gm (51mmol) of dimethylterephthalate, and 30 ml of anhydrous tetrahydrofuranwere mixed with stirring under nitrogen stream, and the refluxing underheat was continued for 4 hours. The refluxing under heat was kept foranother 3 hours while adding dropwise 4.4 gm (51 mmol) of dimethylacetoamide. After cooling the reaction mixture, 65 ml of 2N aqueoushydrochloric acid was added, and the mixture was extracted withchloroform. The extract was dried over anhydrous sodium sulfate and thesolvent was removed by evaporation to give a crude product. Acetone wasadded to the crude product, and recrystallization afforded 6.9 gm of thetarget compound as pale yellow crystals (yield: 43%).

Melting Point: 158.7°-160.1° C.

IR(ν_(KBr), cm⁻¹): 3010, 1610, 1503, 1368, 1290, 1164, 1116.

¹ H-NMR(CDCl₃, δ): 1.29(9H, s), 3.10(6H, bs), 4.15(0.3H, s), 5.88(0.7H,s), 6.35(1H, s), 7.78-8.10(4H, m)

Example 14 Synthesis of1-[5-(1,3-dioxaindanyl)]-4,4-dimethyl-pentane-1,3-dione

Into a 500 ml three-necked flask equipped with a stirrer, a droppingfunnel, a reflux condenser, and a nitogen-inlet tube, were charged 20.13gm (0.50 mol) of 60% sodium hydride and 44.70 gm (0.248 mol) of methylpiperonylate. The mixture was dispersed in 200 ml of tetrahydrofuran andheated under refluxing. To the mixture was dropwise added 25.0 gm (0.25mol) of pinacolone and the mixture was heated with stirring for 3 hours.After cooling, 100 ml of IN hydrochloric acid was added to the reactionmixture, and the organic layer was extracted twice with chloroform. Theextract was thoroughly washed with water and dried over anhydrousmagnesium sulfate and the solvent was removed by evaporation. Theresidue was submitted to silica gel column chromatography using ahexane-ethyl acetate (20:1) mixed solvent as an eluent, followed byevaporation of the solvent in vacuo (126°-128128° C./0.02 mmHg) toproduce 47.90 gm (yield: 78%) of the target compound as an yellow oil.The yellow oily product solidified when left overnight at roomtemperature. The solid was recrystallized from hexane to give colorlesspillar-shaped crystals.

Melting Point: 48.7° C.

IR(ν_(KBr), cm⁻¹): 2970, 2910, 1600, 1510, 1490, 1460, 1350, 1290, 1260,1220, 1130, 1110, 1040, 970, 930, 910, 790.

¹ H-NMR(CDCl₄, δ): 1.29(9H, s, t-C₄ H₉), 5.93(2H, s, --O--CH₂ --O--),6.01(1H, s), 6.70(1H, d, J=8Hz, Aromatic), 7.78-8.35(3H, m, Aromatic),14.83(2H, bs),

Example 15

Synthesis of 1-(3-dimethylaminophenyl)-4,4-dimethylpentane-1,3-dione

Into a 100 ml three-necked flask equipped with a stirrer, a droppingfunnel, a reflux condenser, and a nitogen-inlet tube, were charged 2.08gm (31 mmol) of 60% sodium hydride and 5.0 gm (26 mmol) of ethyl3-dimethylaminobenzoate. The mixture was dispersed in 40 ml oftetrahydrofuran and heated under refluxing. To the mixture was dropwiseadded 3.0 gm (30 mmol) of pinacolone and the mixture was heated withstirring for 3 hours. After cooling, 50 ml of 1N hydrochloric acid wasadded to the reaction mixture, and the organic layer was extracted twicewith chloroform. The extract was thoroughly washed with water and driedover anhydrous magnesium sulfate. The solvent was removed by evaporationto obtain an yellow oil. The oily substance was submitted to theKugelrohr distillation at 200° C., 1 mmHg, and crystallized from hexaneto give 4.81 gm (yield: 75%) of yellow solid product.

¹ H-NMR(CDCl₄, δ): 1.39(9H, s, t--C₄ H₉), 2.99(6H, s, N-CH₃), 6.31(1H,s), 6.90(1H, dd, J=3Hz, 12Hz, Aromatic), 7.25-7.41(3H, m, Aromatic),16.26(1H, bs),

Example 16

Synthesis of 1-(4-dimethylaminophenyl)-4,4-dimethylpentane-1,3-dione

Into a 100 ml three-necked flask equipped with a stirrer, a droppingfunnel, a reflux condenser, and a nitogen-inlet tube, were charged 2.08gm (31 mmol) of 60% sodium hydride and 5.0 gm (26 mmol) of ethyl4-dimethylaminobenzoate. The mixture was dispersed in 40 ml oftetrahydrofuran and heated under refluxing. To the mixture was dropwiseadded 3.0 gm (30 mmol) of pinacolone and the mixture was heated withstirring for 3 hours. After cooling, 50 ml of 1N hydrochloric acid wasadded to the reaction mixture, and the organic layer was extracted twicewith chloroform. The extract was thoroughly washed with water and driedover anhydrous magnesium sulfate. The solvent was removed by evaporationto obtain an yellow oil. The oily substance was submitted to theKugelrohr distillation 150° C., 1 mmHg, and crystallized from hexane togive 4.5 gm (yield: 70%) of yellow solid product.

Melting Point: 61.5°-61.8° C.

IR(ν_(KBr), cm⁻¹): 2960, 2940, 1610, 1570, 1520, 1440, 1380, 1300, 1190,1130, 1070, 1030, 930, 850, 830, 800, 720, 690, 600.

¹ H-NMR(CDCl₄, δ): 1.23(9H, s, t-C₄ H₉), 3.03(6H, s, N-CH₃), 6.20(1H,s), 6.65(2H, d, J=9Hz, Aromatic), 7.83(2H, d, J=9Hz, Aromatic),16.87(1H, bs).

Example 17 Synthesis of1-(4-allyloxy-3-methoxyphenyl)-4,4-dimethylpentane-1,3-dione (1)Synthesis of 4-allyloxy-3-methoxyacetophenone

Into a 1,000 ml three-necked flask equipped with a stirrer, a droppingfunnel, a reflux condenser, and a nitogen-inlet tube, were charged 300ml of tetrahydrofuran, 150 gm (0.90 mol) of acetovanilone, and 149.3 gm(1.08 mol) of potassium carbonate. The mixture was heated underrefluxing while vigorously stirring. To this was dropwise added 131.1 gm(1.08 mol) of allyl bromide. After the addition, the stirring wascontinued overnight. Then, a mixture of 131.1 gm (1.08 mol) of allylbromide and 100 ml of dimethylformamide was added, and the reaction wasfurther continued for 8 hours under refluxing. After cooling, the solidwas collected from the reaction mixture by filtration, thoroughly washedwith 1,000 ml of dichloromethane, and combined with the filtrate. Theorganic layer was washed with 50 ml of 2N hydrochloric acid and 800 mlof water, and dried over anhydrous magnesium sulfate. Magnesium sulfatewas removed by filtration and the solvent evaporated to obtain a brownoil. The oil was submitted to silica gel column chromatography using ahexane-ethyl acetate (2:1) mixed solvent as an eluent to produce 174.8gm (yield: 94%) of the title compound as an yellow oil.

IR(ν_(KBr), cm⁻¹): 3090, 3000, 2940, 2880, 1740, 1680, 1590, 1510, 1470,1420, 1360, 1270, 1220, 1180, 1150, 1080, 1020, 1000, 930, 880, 810,640, 570.

(2) Synthesis of1-(4-allyloxy-3-methoxyphenyl)-4,4-dimethylpentane-1,3-dione

Into a 1,000 ml three-necked flask equipped with a stirrer, a droppingfunnel, a reflux condenser, and a nitogen-inlet tube, was charged 200 mlof tetrahydrofuran. To this was added and dispersed 24 gm (0.6 mmol) of60% sodium hydride and the dispersion was heated under refluxing. To themixture was added dropwise a solution of 61.9 gm (0.3 mol) of4-allyloxy-3-methoxyacetophenone and 39.1 gm (0.3 mol) of ethyl pivalatein 200 ml of tetrahydrofuran over 5 hours. After the addition, themixture was heated with stirring overnight and then ice-cooled. 300 mlof 1N hydrochloric acid was added to the reaction mixture, and theresulting organic layer was washed twice with 100 ml of saturated brineand dried over anhydrous magnesium sulfate. The solvent was removed byevaporation to obtain a brown oil. The oil was submitted to silica gelcolumn chromatography using a hexane-ethyl acetate (2:1) mixed solventas an eluent to produce 74.6 gm (yield: 86%) of the title compound as alight red oil.

Melting Point: 40.0° C.

IR(ν_(KB) r, cm⁻¹): 3090, 2960, 2930, 2870, 2620, 1710, 1680, 1600,1520, 1470, 1430, 1370, 1340, 1280, 1210, 1180, 1150, 1140, 1080, 1020,1,000, 930, 880, 730, 640, 620, 570, 480.

¹ H-NMR(CDCl₄, δ): 1.23(9H, s, t--C₄ H₉), 3.83(3H, s, O--CH₃), 4.43-4.60(2H, m, O--CH₂), 5.06-5.50(2H, m, allylic--CH₂), 5.70-6.10(1H, s,allylic--CH), 6.05(1H, s), 6.67(1H, d, J=9Hz, Aromatic), 7.17-7.32(2H,m, Aromatic), 16.76(1H, bs).

Example 18 Synthesis of1-(3-methoxy-4-propoxyphenyl)-4,4-dimethylpentane-1,3-dione

Into a 50 ml egg plant type flask equipped with a magnetic stirrer, adropping funnel, a reflux condenser, and a nitogen-inlet tube, werecharged 250 mg of 5% palladium/carbon and 5.0 gm (24 mmol) of1-(4-allyloxy-3-methoxyphenyl)- 4,4-dimethylpentane-1,3-dione which hadbeen dispersed in 25 ml of ethanol. After completely replacing thereaction atmosphere by hydrogen, the mixture was stirred for 2 hours atroom temperature. Palladium/carbon was removed by filtration and thesolvent was evaporated to obtain pale yellow oily product. The oil wassubmitted to silica gel column chromatography using a hexane-ethylacetate (10:1-5:1) mixed solvent as an eluent to produce 4.0 gm (yield:80%) of the title compound as a colorless solid.

Melting Point: 55.5°-56.7° C.

IR(ν_(KBr), cm⁻¹): 3090, 2970, 2940, 2880, 1660, 1520, 1470, 1390, 1300,1270, 1220, 1180, 1150, 1140, 1070, 1030, 970, 940, 880, 800, 730.

¹ H-NMR(CDCl₃, δ): 1.06(3H, t, J=3Hz, CH₃), 1.25(9H, s, t--C₄ H₉),1.81-2.00(2H, m, CH₂), 3.93(3H, s, O--CH₃), 4.04(2H, t, J=7Hz, O--CH₂),6.24(1H, s), 6.86-6.91(1H, m, Aromatic), 7.45-7.55(2H, m, Aromatic),16.76(1H, bs).

Experimental Example 1 UV-ray absorbing effect of the compounds of thepresent invention

The absorbance as the UV-ray absorbing effect was measured on theInvention Compounds (Ia)-(Ie) prepared in Examples 1-4 and 6, InventionCompound (If)-(Il) prepared in Examples 7-13, and Comparative Compoundsshown below according to the method described below. The results areshown in Table 1.

Invention Compound

(Ia): 3,4-dimethoxy(4,4-dimethyl-3-oxopentanoyl)benzene

(Ib): 3,4,5-trimethoxy(4-4-dimethyl-3-oxopentanoyl)benzene

(Ic): 1,4-bis(4,4-dimethyl-3-oxopentanoyl)benzene

(Id): 1,3-bis(4,4-dimethyl-3-oxopentanoyl)benzene

(Ie): 2,6-bis(4,4-dimethyl-3-oxopentanoyl)naphthalene

(If): 1,4-bis(4-methyl-3-oxopentanoyl)benzene

(Ig): 1,4-bis(3-oxopentanoyl)benzene

(Ih): 1,4-bis(3-oxododecanoyl)benzene

(Ii): 1,3,5-tris(4,4-dimethyl-3-oxopentanoyl)benzene

(Ij): 1,4-bis(4-hydroxy-4-methyl-3-oxopentanoyl)benzene

(Ik): 1,4-bis(4-methyl-3-oxo-4-azapentanoyl)benzene

(Il):1-(4-methyl-3-oxo-4-azapentanoyl)-4-(4,4-dimethyl-3-oxopentanoyl)benzene

Comparative Compound

1. 2-hydroxy-4-methoxybenzophenone (commercial UV-A absorber)

2.2-ethylhexyl p-methoxycinnamate (commercial UV-B absorber)

Measuring method

Ethanol solutions of each Invention Compound and Comparative Compoundwere prepared (concentration: 2.5×10⁻⁵ mol/l , ethanol: 99.5% reagent,Special grade). Each solution was injected in a quartz cell (1 cm×1 cm)and its absorbance was measured using an automatic recordingspectrophotometer (U-3410 model; manufactured by Hitachi, Ltd.).

                                      TABLE 1                                     __________________________________________________________________________    (UV-ray absorbing effect)                                                                                                 Comparative                       Wavelength                                                                           Invention Compound                   Compound                          (nm)   Ia Ib Ic Id Ie If Ig Ih Ii Ij Ik Il  1   2                             __________________________________________________________________________    290    0.24                                                                             0.25                                                                             0.27                                                                             0.54                                                                             0.44                                                                             0.23                                                                             0.23                                                                             0.24                                                                             0.51                                                                             0.28                                                                             0.28                                                                             0.26                                                                              0.40                                                                              0.54                          300    0.29                                                                             0.36                                                                             0.38                                                                             0.74                                                                             0.29                                                                             0.34                                                                             0.34                                                                             0.34                                                                             0.71                                                                             0.41                                                                             0.37                                                                             0.36                                                                              0.28                                                                              0.60                          310    0.37                                                                             0.46                                                                             0.49                                                                             0.85                                                                             0.43                                                                             0.45                                                                             0.43                                                                             0.44                                                                             0.87                                                                             0.60                                                                             0.49                                                                             0.47                                                                              0.24                                                                              0.64                          320    0.49                                                                             0.52                                                                             0.62                                                                             0.84                                                                             0.55                                                                             0.57                                                                             0.54                                                                             0.59                                                                             0.89                                                                             0.78                                                                             0.57                                                                             0.56                                                                              0.25                                                                              0.52                          330    0.57                                                                             0.51                                                                             0.78                                                                             0.70                                                                             0.75                                                                             0.71                                                                             0.66                                                                             0.75                                                                             0.75                                                                             0.98                                                                             0.61                                                                             0.65                                                                              0.25                                                                              0.27                          340    0.55                                                                             0.43                                                                             0.87                                                                             0.44                                                                             0.91                                                                             0.81                                                                             0.75                                                                             0.85                                                                             0.56                                                                             0.99                                                                             0.57                                                                             0.66                                                                              0.21                                                                              0.08                          350    0.38                                                                             0.24                                                                             0.83                                                                             0.21                                                                             0.97                                                                             0.79                                                                             0.73                                                                             0.84                                                                             0.30                                                                             0.98                                                                             0.45                                                                             0.59                                                                              0.13                                                                              0.02                          360    0.21                                                                             0.13                                                                             0.68                                                                             0.05                                                                             0.88                                                                             0.67                                                                             0.64                                                                             0.71                                                                             0.12                                                                             0.61                                                                             0.29                                                                             0.44                                                                              0.06                                                                              0.01                          370    0.06                                                                             0.03                                                                             0.40                                                                             0.01                                                                             0.73                                                                             0.45                                                                             0.45                                                                             0.46                                                                             0.01                                                                             0.45                                                                             0.15                                                                             0.28                                                                              0.03                                                                              0                             380    0.01                                                                             0.01                                                                             0.20                                                                             0  0.55                                                                             0.26                                                                             0.31                                                                             0.26                                                                             0  0.08                                                                             0.05                                                                             0.13                                                                              0.01                                                                              0                             390    0  0  0.30                                                                             0  0.26                                                                             0.06                                                                             0.16                                                                             0.06                                                                             0  0.02                                                                             0.01                                                                             0.03                                                                              0   0                             400    0  0  0.01                                                                             0  0.09                                                                             0.02                                                                             0.10                                                                             0.01                                                                             0  0.01                                                                             0  0.01                                                                              0   0                             __________________________________________________________________________

As clearly shown in Table 1, the compounds of the present inventionpossess UV-A and UV-B absorbing effects higher than conventionalcompounds, 2-hydroxy-4-methoxybenzophenone and2-ethylhexyl-p-methoxycinnamate. This is the evidence that the compoundsof the present invention exhibit a superior sunscreening effect.

Experimental Example 2

Stability of the compound of the present invention against UV-rays

Experiment procedure

Each of the Invention Compounds or the Comparative Compounds wasdissolved in a 99.5% ethanol/distilled water (3/2) solvent to prepare 2mmol/lconcentration solutions. Onto the solution UV-ray was irradiatedfor 14 hours using a xenon fading tester having a similar wave lengthand strength as those of sun light. After the solvent was evaporated,each sample was subjected to quantitative analysis for measuring theresidual rate of the composition to determine the stability againstlight of each composition. The results are shown in Table 2.

                  TABLE 2                                                         ______________________________________                                        (Stability against light)                                                                   Residual rate (%)                                                             Hours after start of                                                          irradiation                                                     Compound        14 hours 65 hours                                             ______________________________________                                        Invention                                                                     Composition                                                                   Ia              >99      99                                                   Ib              >99      99                                                   Ic              99       96                                                   Id              99       95                                                   Ie              99       95                                                   If              99       94                                                   Ig              99       94                                                   Ih              99       95                                                   Ii              99       96                                                   Ij              99       95                                                   Ik              97       92                                                   Il              96       92                                                   Comparative                                                                   Composition                                                                   2               42       10                                                   3*              73       29                                                   ______________________________________                                         *Comparative Composition 3: 4methoxy-4t-butyl-benzoylmethane             

From the results in Table 2, the compounds of the present inventionapparently have an outstanding stability against UV-rays in comparisonwith 4-methoxy-4'-t-butyldibenzoyl-methane and2-ethylhexyl-p-methoxycinnamate which are known as a general UV-Aabsorbing agent and UV-B absorbing agent respectively.

Example 19 O/W cream

The following components were formulated according to a known method toprepare O/W creams.

    ______________________________________                                        <Formulation>       Wt %                                                      ______________________________________                                        Invention Compounds (Ia)-(Il)                                                                     2.0                                                       Stearic acid        1.0                                                       Lipophilic-type monostearic                                                                       2.0                                                       acid glyceride                                                                Polyoxyethylenesorbitane                                                                          1.0                                                       monostearate                                                                  Cetyl alcohol       1.0                                                       Stearyl alcohol     1.0                                                       Squalane            10.0                                                      Liquid paraffin     20.0                                                      Vaseline            5.0                                                       Butyl parabene      0.1                                                       Methyl parabene     0.1                                                       Triethanol amine    1.0                                                       Glycerol            10.0`                                                     Perfume             q.s.                                                      Water               Balance                                                   Total               100.0                                                     ______________________________________                                    

Example 20 W/O cream

The following components were formulated according to a known method toprepare W/O creams.

    ______________________________________                                        <Formulation>       Wt %                                                      ______________________________________                                        Invention Compound (Ia)-(Il)                                                                      2.0                                                       Sorbitan sesquioleate                                                                             4.0                                                       Aluminum stearate   0.5                                                       Cetyl alcohol       4.0                                                       Liquid paraffin     16.0                                                      Squalane            10.0                                                      Isopropylmyristate  5.0                                                       Sodium benzoate     0.3                                                       Glycerol            10.0                                                      Perfume             q.s.                                                      Water               Balance                                                   Total               100.0                                                     ______________________________________                                    

Example 21 O/W milky lotion

The following components were formulated according to a known method toprepare O/W milky lotions.

    ______________________________________                                        <Formulation>       Wt %                                                      ______________________________________                                        Invention Compounds (Ia)-(Il)                                                                     3.0                                                       Stearic acid        2.0                                                       Sorbitan monostearate                                                                             1.5                                                       Polyoxyethylenesorbitane                                                                          1.0                                                       monostearate                                                                  Cetyl alcohol       0.4                                                       Stearyl alcohol     0.3                                                       Isopropylmyristate  7.0                                                       Squalane            5.0                                                       Liquid paraffin     5.0                                                       Solid paraffin      2.0                                                       Ethyl parabene      0.1                                                       Methyl parabene     0.1                                                       Carbopole           0.2                                                       Potassium hydroxide 0.4                                                       Perfume             q.s.                                                      Water               Balance                                                   Total               100.0                                                     ______________________________________                                    

Example 22 Toilet lotion

The following components were formulated according to a known method toprepare toilet lotions.

    ______________________________________                                        <Formulation>       Wt %                                                      ______________________________________                                        Invention Compound (Ia)-(Il)                                                                      2.0                                                       Polyoxyethylene(23 EO)                                                                            4.0                                                       lauryl ether                                                                  Ethanol             10.0                                                      Glycerol            3.0                                                       Dipropylene glycol  7.0                                                       Lactic acid          0.05                                                     Sodium lactate       0.12                                                     Methyl parabene     0.1                                                       Perfume             q.s.                                                      Pigment             Small amount                                              Water               Balance                                                   Total               100.0                                                     ______________________________________                                    

The aroyl ketone derivative (I) of the present invention can provide anexcellent UV-ray absorbing effect and has an outstanding stabilityagainst light. Thus the UV-ray absorber or cosmetic compositioncontaining the aroyl ketone derivative (I) can exhibit an excellentsunscreening effect.

What is claimed is:
 1. An aroyl ketone derivative represented by theformula (I):

    Ar(COCH.sub.2 COR.sup.1).sub.n

where R¹ represents t-butyl or heptyl, Ar represents a benzene ornaphthalene ring which is substituted with one or more alkoxy groupshaving 1-24 carbon atoms, alkenyloxy groups having 1-24 carbon atoms,mono- or di-alkylamino-groups having 1-24 carbon atoms, orα-methylenedioxy groups and n is an integer of 1-3; excluding thecompounds where Ar is a di- or tri-methoxy substituted benzene ring andcompounds represented by the following formulae: ##STR6##
 2. An aroylketone derivative represented by the formula (I):

    Ar(COCH.sub.2 COR.sup.1).sub.n

wherein R¹ represents t-butyl or heptyl, Ar represents a benzene ornaphthalene ring which is substituted with one or more mono- ordi-alkylamino groups having 1-24 carbon atoms and n denotes an integerof 1-3.